Reaction of β-aminopropionohydroxamic acid with aldehydes and ketones

Article abstract of DOI:10.1007/BF02495976

β-Aminopropionohydroxamic acid reacts with aliphatic aldehydes or ketones to give 2-substituted 1-hydroxytetrahydropyrimidin-6-ones, while its reaction with aromatic carbonyl compounds leads to either the same products or Schiff's bases, which can exist in tautomeric equilibrium in solution.